| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:75646694-75646908 | Common:1; Rare:74 | ||||
| chr2:75710669-75710775 | Common:2; Rare:41 | ||||
| chr2:77522218-77522423 | Rare:30 | ||||
| chr2:80304182-80304311 | Rare:32 | ||||
| chr2:80304410-80304631 | Common:1; Rare:44 | ||||
| chr2:80305005-80305131 | Common:1; Rare:17 | ||||
| chr2:84459219-84459587 | Common:3; Rare:93; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:84516303-84516571 | Common:1; Rare:71 | ||||
| chr2:84904912-84905347 | Common:2; Rare:86 | ||||
| chr2:84905527-84905980 | Common:1; Rare:132 | ||||
| chr2:85327916-85328094 | Common:3; Rare:80 | ||||
| chr2:85354526-85354807 | Common:1; Rare:93 | ||||
| chr2:85539072-85539244 | Common:3; Rare:90 | ||||
| chr2:85561421-85561631 | Common:1; Rare:71; Clinvar:4 | ||||
| chr2:85595546-85595782 | Common:2; Rare:76 |